50690-52-3

Upstream product

• 14191-95-8 4-cyanomethylphenol 
• 13435-20-6 tetraethylammoniumcyanide 
• 40141-11-5 (4-chloromethyl-phenyl)-propyl ether 
• 106-94-5 propyl bromide 
• 90925-43-2 4-n-propyloxybenzyl alcohol 
• 5736-85-6 4-propoxybenzaldehyde 

Downstream Products

• 26118-57-0 2-(4-(n-propoxy)phenyl)acetic acid 
• 57224-67-6 4-propoxy-phenethylamine 
• 23528-50-9 1-Cyano-1-(4-n-propoxyphenyl)-cyclopentan 
• 74205-07-5 1-(4-Propoxy-phenyl)-cyclopropanecarbonitrile 
• 74205-21-3 1-(4-Propoxy-phenyl)-cyclobutanecarbonitrile 
• 132372-81-7 5-(4-Propoxybenzyl)-1H-tetrazole 
• 89790-02-3 2-(4-Propoxy-phenyl)-acetamide 
• 100794-58-9 3-chloro-propionic acid-(4-propoxy-phenethylamide) 
• 132372-98-6 [5-(4-Propoxy-benzyl)-tetrazol-2-yl]-acetic acid 
• 132372-89-5 [5-(4-Propoxy-benzyl)-tetrazol-1-yl]-acetic acid 
• 61492-13-5 (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-{[1-(4-propoxy-phenyl)-cyclopentanecarbonyl]-amino}-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 61492-45-3 (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-{[1-(4-propoxy-phenyl)-cyclobutanecarbonyl]-amino}-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 61492-29-3 (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-{[1-(4-propoxy-phenyl)-cyclopropanecarbonyl]-amino}-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 

Relevant academic research and scientific papers

Synthesis and thermal properties of twin dimers containing cyanostilbene derivatives as a mesogenic group

We synthesized twin dimers (TDs) with different linking groups between a mesogenic group and a flexible spacer, different spacer length, and different terminal alkyl chain length to clarify the effect of these groups on the mesomorphic properties of the T

Design, synthesis and antiproliferative activity of tripentones: A new series of antitubulin agents

Structure-activity relationship studies of a new series of tripentones (thieno[2,3-b]pyrrolizin-8-ones), led us to prepare several derivatives with antiproliferative activities. The most promising 3-(3-hydroxy-4-methoxyphenyl)thieno[2,3-b]pyrrolizin-8-one 20 (leukemia L1210, IC50 = 15 nM) was shown to be a potent inhibitor of tubulin polymerization.

Design of Inhibitors from the Three-Dimensional Structure of Alcohol Dehydrogenase. Chemical Synthesis and Enzymatic Properties

Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.